5C51.2 Disorders of glyoxylate metabolism

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01

Primary hyperoxaluria, or oxalosis, is a rare metabolic disorder transmitted as an autosomal recessive disease, including both type 1, the most frequent, and type 2, extremely rare. Hyperoxaluria type 1 is due to a defect of the peroxysomal hepatic enzyme L-alanine: glyoxylate aminotransferase (AGT). Hyperoxaluria type 2 is extremely rare and is due to glycerate dehydrogenase deficiency.

sections/codes in this section (5C51.2-5C51.2)

• Primary hyperoxaluria type 1  (5C51.20)
• Other specified disorders of glyoxylate metabolism  (5C51.2Y)
• Disorders of glyoxylate metabolism, unspecified  (5C51.2Z)

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